Kurtis is 14 years old. He loves music and video games, but he dreams of becoming a professional basketball player. When he’s not a school, you can find him on the court practicing with his AAU team, Texas Explosion!
“People flock to him, he has that unique quality. If you know him, you want to be with him. Even grownups take to him,” says his mom, Brandie. “I see leadership.” She describes Kurtis as animated, personable, and fun. Even when playing on-line video games, 12-year-old Kurtis breaks into song, dances, and even talks with a fake British accent. He loves basketball and plays on two different teams. His coaches say even after playing for less than two years, he is really going to be someone on the court. Kurtis stands out on the court for two reasons; first, he is really good at basketball and second, he has vitiligo.
Vitiligo is considered to be an autoimmune condition where the body destroys the pigment cells which causes white patches on the skin. It is typically a chronic condition that can significantly alter a person’s appearance. While there are treatments, they are often of limited effectiveness and there are no known cures.
Kurtis started developing light spots on his skin when he was just six months old. Until about the time he started kindergarten, the spots were only on his arms and legs, and could be covered with long sleeves and pants. Then they began appearing on his face.
“Kurtis taught me a lesson about covering them. He ran into school that first day, and we haven’t covered them since,” Brandie said. He was so excited to let his true self shine through. She said his outgoing personality helps him with other people’s stares and questions. Even if they don’t feel like they need to shield him from this, they also realize no child is immune to being hurt.
A Children’s House for the Soul offers a warm accepting place to learn ways to empower children and teens facing their own unique challenges. Kurtis and his family attended the “Love the Skin You’re In” conference, and he has been to Camp Dermadillo several times.
Brandie said when they woke up the morning of the conference they almost decided not to come, but wanted to see what it was all about. She is so glad they did. “It’s not as big a deal at conferences or camp, there are no mean looks or stares, there is a comfort level, without judgment,” she explained.
Even with his outgoing and entertaining personality, Kurtis doesn’t always know how to answer questions or respond to people staring at him, he just wants to be accepted and make friends. His mom knows he hears the questions and she tries to give him the tools necessary to respond. A Children’s House for the Soul can help.
We had an amazing time celebrating the launch of our brand new SKIN DISCOVERY BOXES, a very special collaboration with our friends at CeraVe! CeraVe’s tireless pursuit of therapeutic skincare for all is truly more than skin deep and we couldn’t be more thankful. We celebrated in style thanks to our friends at Star Cinema …
A Children’s House for the Soul believes that it takes a village to support a child and family impacted by skin disease and birthmarks and that we are all better together.
Open House and Ribbon Cutting/Bring A Children’s House Home: On June 5th we began a very exciting new chapter of our A Children’s House story in the form of opening up our new beautiful space to serve children and teenagers with skin conditions and birthmarks and their families. This space includes a salon, a library & craft space, a teen room, and more! We also debuted our incredible new custom mural from up and coming local artist Eli Pallaert.
Our Family Trivia night was oh so much fun, and a huge success! We had so much fun getting to reconnect with all our friends and enjoy some laughs while snacking out on pizza and snowcones!
In honor of Vascular Birthmark Awareness Month, our childlife specialist Lindsay O’Sullivan had a great conversation with Jose about growing up with his special masterpiece skin!
In this interview, Ally shares about her experiences growing up with Ichthyosis. Ally shares how: Meeting other kids with special skin can help kids to feel less isolated and give them a very special sense of comradery and understanding. Parents don’t have to do everything perfectly to be the perfect parent for their child and …
What a wonderful time to relax, enjoy friendly company, and share their hearts on being a mama to a kiddo or teen with special skin. It was truly so special! These mamas were made a masterpiece!
Vascular birthmarks are very common in children. These birthmarks are made of blood vessels in the skin and can occur anywhere on the body. They may be pink or red in color, blue or purplish, flat or raised. Since they are vascular, sometimes they will feel warm to touch and may change in color with …
We have some exciting updates about our Capital Campaign! Learn about our short and long term plans for our own space.
You Can’t Teach What Has No History “This is how much God loved the world: He gave his Son, his one and only Son. And this is why: so that no one need be destroyed; by believing in him, anyone can have a whole and lasting life. God didn’t go to all the trouble of …
In honor of Ectodermal Dysplasia Awareness month in February, we sat down with two of our dearest friends Zach and his mama Susan! Zach is an avid golfer, an Aggie, and is affected by Ectodermal Dysplasia. Susan and Zach teach us about ED and the importance of finding community. They also had helpful tips and …
Join us for a fun and inspiring interview with this incredible lady Ana Maria! Ana Maria Triana is 15 years old and the author of How to Conquer Alopecia Universalis. Ana Maria gives heartfelt advice, shares wisdom beyond her years, and will leave you feeling full of compassion and confidence. A Children’s House for the …
In honor of the upcoming National Epidermolysis Bullosa (EB) Awareness week, we wanted to share this great piece from our friend, Rachael Wrobel about how her mama mothered her well, even despite the challenges of EB.
I am fortunate enough to be Mama to three little girls. Shortly after my eldest daughter’s first birthday (about 4 years ago) I noticed her hair was thinning. I was told by many it was just typical baby hair loss until it just couldn’t be described at “typical” any longer.
After the last several months of this pandemic, I think we are all well-versed in how important it is to wash our hands so that we don’t spread germs. But with all this hand washing and sanitizing, dry skin, eczema breakouts, and contact dermatitis have become even more troublesome. What can we do about it?
Join us for a quick and very insightful video interview with Dr. Alana Kennedy-Nasser as she shares with us how to keep kids safe as they go back to school in-person and how to keep kids developmentally “on track” as they attend school virtually.
What questions do you have for back to school content experts? Read on for some brilliant questions and answers from this super smart teacher mama, Lacy Cunningham, M.A.Ed.
Online learning can be a fun experience filled with lots of great experiences; but as humans, we were meant to interact with one another and have companionship. How can we develop ways to ensure kids stay engaged while learning in a different setting?
This year, the normal first day of school jitters will likely be accompanied by some new concerns that we have not encountered before. Lindsey O’Sullivan, Child Life Specialist, provides guidance on how to navigate these conversations with your child.
As we prepare for school to begin, those of us that are sending our kiddos slowly back out into the world may find ourselves explaining what has changed (again) in the last few months. Dr. Chad Brandt, a therapist who specializes in anxiety in children and teens, offers us a few guideposts for talking about the coronavirus with children.